DERMOGEN

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: DERMOGEN
Generic name: ZINC OXIDE
Manufacturer: KRAMER NOVIS
Product type: HUMAN OTC DRUG
SPL set ID: 38e02d1c-c143-4da6-ad32-a3ce2861aac5
SPL ID: 2a461bfd-7006-4b64-addf-474ee1fbd48f
Version: 3
Effective date: 2025-11-14
Source export date: 2026-09-28
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:05:16

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M016	openfda.application_number
brand name		DERMOGEN	openfda.brand_name
generic name		ZINC OXIDE	openfda.generic_name
manufacturer name		KRAMER NOVIS	openfda.manufacturer_name
ndc	package	52083-680-04	openfda.package_ndc
ndc	product	52083-680	openfda.product_ndc
ndc11	package	52083068004	derived:openfda.package_ndc
rxcui		1793915	openfda.rxcui
spl id		2a461bfd-7006-4b64-addf-474ee1fbd48f	id
spl set id		38e02d1c-c143-4da6-ad32-a3ce2861aac5	set_id
unii		SOI2LOH54Z	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warning • For external use only. When using this product • do not get into eyes Stop and ask a doctor if • condition worsens • symptoms lasts more than 7 days or clear up and occur again within a few days Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.